Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,419 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,419 in last 12 months

Showing 3466134680 of 49,150 recalls

Medical DeviceJanuary 18, 2016· Philips Respironics

Recalled Item: Trilogy 100 Recalled by Philips Respironics Due to Software Issue

The Issue: Software Issue

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Amerisource Health Services

Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...

The Issue: Failed Dissolution Specifications: Unexplained low out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 15, 2016· Master Herbs, Inc./Li

Recalled Item: Licorice Coughing Liquid (guaifenesin) Recalled by Master Herbs, Inc./Li Due...

The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2016· Spectranetics Corp.

Recalled Item: 2.3mm Turbo-Power OTW Recalled by Spectranetics Corp. Due to The product is...

The Issue: The product is labeled with an expiration date that is past its shelf life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2016· Mako Surgical Corporation

Recalled Item: Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for...

The Issue: Reports where the Mylar/Tyvek pouch for RESTORIS MCK Baseplate in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2016· CareFusion 303, Inc.

Recalled Item: Jadak Barcode Scanner Recalled by CareFusion 303, Inc. Due to Customers...

The Issue: Customers reported issues when scanning medications with the scanners. When...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2016· OraSure Technologies, Inc.

Recalled Item: OraQuick HCV Visual Panel Intended to assist new operation Recalled by...

The Issue: OraSure Technologies, Inc. discovered the package insert included with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJanuary 15, 2016· The Anspach Effort, Inc.

Recalled Item: Universal Battery Charger II (UBC II) Recalled by The Anspach Effort, Inc....

The Issue: The device is reported to enter safe mode and is no longer able to charge...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJanuary 15, 2016· NutraKey, Inc.

Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy

The Issue: Undeclared Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· NutraKey, Inc.

Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy

The Issue: Undeclared Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· NutraKey, Inc.

Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy

The Issue: Undeclared Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· Hain Celestial Group

Recalled Item: Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17...

The Issue: Hain Celestial Seasoning is recalling Celestial Seasonings Roastaroma Herbal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 15, 2016· NutraKey, Inc.

Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy

The Issue: Undeclared Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 14, 2016· BlendTech Inc

Recalled Item: Uncle Buck's Fish Batter Mix Original Recalled by BlendTech Inc Due to...

The Issue: Product contains an undeclared milk ingredient.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 14, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: BCS XP Automated Blood Coagulation Analyzer System Recalled by Siemens...

The Issue: False short clotting times for PT on BCS and BCS XP with Dade Innovin can...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing